K-number	K013705
Device name	ACT III VENTRICULAR CATHETER
Applicant	Innerspace, Inc.
Product code	GWM
Device class	Class II
Decision date	Sep 9, 2002
Decision	Substantially Equivalent
Regulation	882.1620

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View the full FDA submission: accessdata.fda.gov

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ACT III VENTRICULAR CATHETER

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